lafora body การใช้

Lafora bodies have been observed in virtually all organs of patients with the disease.
By contrast, the " abnormal glycogen " in Lafora bodies has an excessive phosphate content and branches at abnormally long intervals.
Astrocytes contribute almost exclusively to brain glycogen storage yet do not develop Lafora bodies, which might highlight the importance of the capacity to degrade glycogen.
In a later study, Lafora disease has been and is now viewed as a neurodegenerative disease, since prior to the actual formation of Lafora bodies there has been seen to be an impairment in the development of cerebral cortical neurons.
"' Lafora disease "', also called "'Lafora progressive myoclonic epilepsy "'or "'MELF "', is a fatal autosomal recessive genetic disorder characterized by the presence of inclusion bodies, known as Lafora bodies, within the cytoplasm of the cells of the heart, liver, muscle, and skin.